A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517365



Internal ID22575329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:2916649..2919849hg38UCSC Ensembl
chrY:2784690..2787890hg19UCSC Ensembl
CytobandYp11.31
Allele length
AssemblyAllele length
hg383201
hg193201
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970024
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517365
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer